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Dictionary » Camurati-Engelmann Syndrome
 

Camurati-Engelmann Syndrome

Introduction: Camurati-Engelmann Syndrome

Description of Camurati-Engelmann Syndrome

Camurati-Engelmann Syndrome: An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder.
Source: MeSH 2007

Camurati-Engelmann Syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Camurati-Engelmann Syndrome:

Terms associated with Camurati-Engelmann Syndrome:

Terms Similar to Camurati-Engelmann Syndrome:

  • Diaphyseal Dysplasia, Progressive
  • Engelmann's Disease

Source - MeSH 2007

Broader terms for Camurati-Engelmann Syndrome

Source - MeSH 2007

Hierarchical classifications of Camurati-Engelmann Syndrome

The following list attempts to classify Camurati-Engelmann Syndrome into categories where each line is subset of the next.

MeSH 2007 Hierarchy:

MeSH 2007 Hierarchy

Interesting Medical Articles:

Medical dictionaries:

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